GPX3, glutathione peroxidase 3, 2878

N. diseases: 156; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3828599
rs3828599
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0020557
Disease:
Hypertriglyceridemia
0.010 GeneticVariation BEFREE Gene polymorphisms: <i>SOD2</i> rs4880, <i>SOD3</i> rs2536512 and rs2855262, <i>GPX</i> rs3828599, and <i>GSTT1</i> (deletion) were evaluated the associations with HTG, low HDL-C, high TG/HDL-C ratio, and severity of coronary atherosclerosis. 31396447 2019
dbSNP: rs3828599
rs3828599
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Gene polymorphisms: <i>SOD2</i> rs4880, <i>SOD3</i> rs2536512 and rs2855262, <i>GPX</i> rs3828599, and <i>GSTT1</i> (deletion) were evaluated the associations with HTG, low HDL-C, high TG/HDL-C ratio, and severity of coronary atherosclerosis. 31396447 2019
dbSNP: rs3805435
rs3805435
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C4275242
Disease:
Sudden sensorineural hearing loss
0.010 GeneticVariation BEFREE As the result, the AG genotype of rs3805435 had an adjusted odds ratio (OR) of 0.54 (95% confidence interval = 0.37-0.79, p = 0.001) compared with the AA genotype in the SSNHL cases. 28738977 2017
dbSNP: rs8177441
rs8177441
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE By using the LRMW method, three variants (fetal rs625879, maternal rs2169650, and maternal rs8177441) were identified with a joint association to CHD risk (nominal P-value = 1.13e-07). 26612412 2016
dbSNP: rs8177409
rs8177409
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE This study shows that serum levels of GPx3 are increased in subjects with MetS and that rs8177409 SNP was associated with cardiovascular risk in a Mexican population. 24819036 2014
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Four SNPs (GPX3 rs2070593, rsGPX4 rs2074451, SELS rs9874, and TXNRD1 rs17202060) significantly interacted with dietary oxidative balance score after adjustment for multiple comparisons to alter breast cancer risk. 24278290 2013
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Four SNPs (GPX3 rs2070593, rsGPX4 rs2074451, SELS rs9874, and TXNRD1 rs17202060) significantly interacted with dietary oxidative balance score after adjustment for multiple comparisons to alter breast cancer risk. 24278290 2013
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C0085580
Disease:
Essential Hypertension
0.010 GeneticVariation BEFREE In the present study we have investigated the association of three single nucleotide polymorphisms in glutathione peroxidase (GPx) genes GPX1 rs1050450 (P198L), GPX3 rs2070593 (G930A) and GPX4 rs713041 (T718C) with the risk of cerebral stroke (CS) in patients with essential hypertension (EH). 22158110 2012
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE In the present study we have investigated the association of three single nucleotide polymorphisms in glutathione peroxidase (GPx) genes GPX1 rs1050450 (P198L), GPX3 rs2070593 (G930A) and GPX4 rs713041 (T718C) with the risk of cerebral stroke (CS) in patients with essential hypertension (EH). 22158110 2012
dbSNP: rs3828599
rs3828599
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE The polymorphism of rs3828599 of GPx-3 gene might be associated with hypertension in rural Han Chinese from Fuxin, Liaoning. 21933611 2011
dbSNP: rs8177412
rs8177412
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0022658
Disease:
Kidney Diseases
0.010 GeneticVariation BEFREE The aim of the present investigation was to test whether functional single nucleotide polymorphisms (SNPs) in genes involved in the generation of NADPH-dependent O₂•⁻ (-675 T → A in CYBA, unregistered) and in glutathione metabolism (-129 C → T in GCLC [rs17883901] and -65 T → C in GPX3 [rs8177412]) confer susceptibility to renal disease in type 1 diabetes patients. 21962117 2011
dbSNP: rs8177412
rs8177412
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C1112433
Disease:
Thromboembolic stroke
0.010 GeneticVariation BEFREE Single-point analysis revealed that the G allele of htSNP rs8177412 was significantly overtransmitted to affected AS children (T/U = 25 : 11, χ(2) = 5.54, P = 0.019), but not to affected TS children (T/U = 49 : 40, χ(2) = 0.91, P = 0.34). 20946167 2011
dbSNP: rs8177412
rs8177412
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation BEFREE The aim of the present investigation was to test whether functional single nucleotide polymorphisms (SNPs) in genes involved in the generation of NADPH-dependent O₂•⁻ (-675 T → A in CYBA, unregistered) and in glutathione metabolism (-129 C → T in GCLC [rs17883901] and -65 T → C in GPX3 [rs8177412]) confer susceptibility to renal disease in type 1 diabetes patients. 21962117 2011
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland
0.010 GeneticVariation BEFREE A total of 6 tSNPs (rs3763013, rs8177412, rs3805435, rs3828599, rs3792796, and rs2070593) of GPX3 were genotyped in Chinese DTC cases (n = 268) and controls (n = 378). 19375609 2009
dbSNP: rs2070593
rs2070593
Entrez Id: 2878
Gene Symbol: GPX3
GPX3
CUI: C1337013
Disease:
Differentiated Thyroid Gland Carcinoma
0.010 GeneticVariation BEFREE A total of 6 tSNPs (rs3763013, rs8177412, rs3805435, rs3828599, rs3792796, and rs2070593) of GPX3 were genotyped in Chinese DTC cases (n = 268) and controls (n = 378). 19375609 2009
dbSNP: rs3805435
rs3805435
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C1337013
Disease:
Differentiated Thyroid Gland Carcinoma
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009
dbSNP: rs3805435
rs3805435
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009
dbSNP: rs3828599
rs3828599
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C1337013
Disease:
Differentiated Thyroid Gland Carcinoma
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009
dbSNP: rs3828599
rs3828599
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009
dbSNP: rs8177412
rs8177412
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C4722172
Disease:
Primary differentiated carcinoma of thyroid gland
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009
dbSNP: rs8177412
rs8177412
Entrez Id: 2878;105378228
Gene Symbol: GPX3;LOC105378228
GPX3;LOC105378228
CUI: C1337013
Disease:
Differentiated Thyroid Gland Carcinoma
0.010 GeneticVariation BEFREE We found that the G allele of rs3805435 or the T allele of rs3828599 may exert a protective effect for DTC in the older population, whereas the C allele of rs8177412 confers an increased risk effect for DTC. 19375609 2009